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panyl10055 离线
性别 | 男 | 年龄 | 68 | 临床诊断 | 间质瘤 |
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一般病史 | 胃粘膜下肿块 | ||||
标本名称 | 胃部分切除标本 | ||||
大体所见 | 粘膜下肿块2*1.8cm,界清,灰白色 |
panyl10055 离线
zyyzwangjin 离线
lantian0508 离线
xiaofeng1008 离线
个人认为还是诊断炎性纤维性息肉合适一些
囊性扩张的腺体,畸形的血管,围绕血管的排列方式,散在的嗜酸性粒细胞,间质的异型细胞等,都更类似于息肉,而不是GIST
一些人诊断GIST可能是因为CD34阳性,但炎性纤维性息肉表达vimentin, CD34, calponin,不表达CD117
附上一点说明:引自《Surgical Pathology of the GI Tract, Liver, Biliary Tract, and Pancreas,
INFLAMMATORY FIBROID POLYP
Clinical Features
Inflammatory fibroid polyps are mesenchymal proliferations composed of a mixture of stromal spindle cells, small blood vessels, and inflammatory cells, particularly eosinophils.[190–192] They may occur anywhere in the GI tract but are most common in the stomach and small intestine. In the stomach, inflammatory fibroid polyps usually occur in the sixth decade of life. Recent studies have reported a disproportionately large number of gastric inflammatory fibroid polyps in female patients.[193], [194] Some have suggested an infectious etiology for inflammatory fibroid polyps.[191], [192] However, no causative agent has ever been identified[195]; thus, most observers currently consider inflammatory fibroid polyps to be a form of reactive pseudotumor. When small, these tumors may be discovered incidentally at endoscopy. However, large lesions may cause obstructive symptoms such as nausea, vomiting, and abdominal pain. In some cases, inflammatory fibroid polyps may contain a long stalk; these may prolapse through the pyloric sphincter and cause obstruction.[196] Some studies suggest that inflammatory fibroid polyps are more common among patients with atrophic gastritis and pernicious anemia.
Pathologic Features
Inflammatory fibroid polyps are typically small, wellcircumscribed, submucosally based, sessile lesions that may show ulceration of the overlying mucosa. Their median size is 1.5cm, and, although most lesions are smaller than 3cm in diameter, polyps that measure as large as 5cm in diameter have been reported. In the stomach, they most commonly arise in the antrum, immediately proximal to, or overlying, the pyloric sphincter.
Microscopically, inflammatory fibroid polyps are submucosal tumors and often show an abrupt demarcation at the level of the muscularis propria. Mucosal involvement is common with gastric lesions. However, unlike small intestinal lesions, involvement of the muscularis propria is unusual in gastric polyps. Extension of the tumor into the mucosa causes separation of gastric glands, which results in a disordered and atrophic appearance. Inflammatory fibroid polyps are composed of a loose mixture of spindle-shaped, plump, cytologically bland stromal cells, inflammatory cells, and small, thin-walled blood vessels in an edematous or myxoid background (Fig. 17-21). In the stomach, stromal cells often proliferate in a concentric fashion around small and medium-sized blood vessels.[197], [198] Mitotic figures are rare but may occasionally be present in deeper portions of the lesion. Atypical mitoses are never present. Eosinophils are a prominent inflammatory component and may also encircle vessels. Larger lesions may show collagen deposition and smooth muscle proliferation, or even giant cell formation.
Immunohistochemically, stromal cells have been reported to be positive for vimentin, CD34, fascin, CD35, cyclin D1, and calponin.[194,197–201] A smaller proportion are also positive for smooth muscle actin, HHF-35, KP-1, and Mac-387.[194,197–201] In contrast to stromal tumors of the GI tract, stromal cells in inflammatory fibroid polyps are negative for CD117 (c-kit).[194], [197] Although the histogenesis of inflammatory fibroid polyps remains controversial, a possible origin in dendritic cells or CD34-positive perivascular cells has been proposed.[194], [201] Differentiating between inflammatory fibroid polyps and inflammatory myofibroblastic tumors is discussed next.